Chapter 415

Laryngotracheal Stenosis and Subglottic Stenosis

Taher Valika, James W. Schroeder Jr

Laryngotracheal stenosis is the second most common cause of stridor in neonates and is the most common cause of airway obstruction requiring tracheostomy in infants. The glottis (vocal cords) and the upper trachea are compromised in most laryngeal stenosis, particularly those that develop following endotracheal intubation. Subglottic stenosis is a narrowing of the subglottic larynx, which is the space extending from the undersurface of the true vocal cords to the inferior margin of the cricoid cartilage. Subglottic stenosis is considered congenital when there is no other apparent cause such as a history of laryngeal trauma or intubation. Approximately 90% of cases manifest in the 1st yr of life. Management relies on fine-tuning the airway, while ensuring the patient continues to grow. Knowledge of preventative measures is imperative to all healthcare members.

415.1

Congenital Subglottic Stenosis

Keywords

  • subglottic stenosis

See Chapter 413.2 .

415.2

Acquired Laryngotracheal Stenosis

Taher Valika, James W. Schroeder Jr

Keywords

  • subglottic stenosis
  • laryngotracheal stenosis

Ninety percent of acquired stenoses are a result of endotracheal intubation. The narrowest portion of the pediatric larynx is the subglottic region due to the narrow cricoid cartilage. When the pressure of the endotracheal tube against the cricoid mucosa is greater than the capillary pressure, ischemia occurs, followed by necrosis and ulceration. Secondary infection and perichondritis develop with exposure of cartilage (Fig. 415.1 ). Granulation tissue forms around the ulcerations. These changes and edema throughout the larynx usually resolve spontaneously after extubation. Chronic edema and fibrous stenosis develop in only a small percentage of cases.

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Fig. 415.1 Bronchoscopy in a 2 mo old infant showing mucosal erosion and cartilage exposure in the subglottic region. Child was intubated with an age-appropriate tube but with an excess of air in cuff. (Courtesy Dr. Taher Valika, Division of Pediatric Otolaryngology, Ann & Robert H. Lurie Children's Hospital of Chicago.)

A number of factors predispose to the development of laryngeal stenosis. Laryngopharyngeal reflux of acid and pepsin from the stomach is known to exacerbate endotracheal tube trauma. More damage is caused in areas left unprotected, owing to loss of mucosa. Congenital subglottic stenosis narrows the larynx which makes the patient more likely to develop acquired subglottic stenosis because significant injury is more likely to occur with use of an endotracheal tube of age-appropriate size. Other risk factors for the development of acquired subglottic stenosis include sepsis, malnutrition, chronic inflammatory disorders, and immunosuppression. An oversized endotracheal tube is the most common factor contributing to laryngeal injury. A tube that allows a small air leak at the end of the inspiratory cycle minimizes potential trauma. Other extrinsic factors—traumatic intubation, multiple reintubations, movement of the endotracheal tube, and duration of intubation—can contribute to varying degrees in individual patients.

Clinical Manifestations

Symptoms of acquired and congenital stenosis are similar. Spasmodic croup, the sudden onset of severe croup in the early morning hours, is usually caused by laryngopharyngeal reflux with transient laryngospasm and subsequent laryngeal edema. These frightening episodes resolve rapidly, often before the family and child reach the emergency department. Other presentations can also involve neonates who fail extubation, despite multiple attempts, and children with permanent dyspnea, stridor, or dysphonia.

Diagnosis

The diagnosis can be made by posteroanterior and lateral airway radiographs. The gold standard to confirm the diagnosis is via direct laryngoscopy and bronchoscopy in the operating room. High-resolution CT imaging and ultrasonography are of limited value. This is similar to the workup associated with congenital subglottic stenosis.

Treatment

The severity, location, and type (cartilaginous or soft tissue) of the stenosis determine the treatment. Mild cases can be managed without operative intervention because the airway will improve as the child grows. Moderate soft tissue stenosis is treated by endoscopy using gentle dilations or CO2 laser. Severe laryngotracheal stenosis is likely to require laryngotracheal reconstructive (expansion) surgery or resection of the narrowed portion of the laryngeal and tracheal airway (cricotracheal resection). Every effort is made to avoid tracheotomy using endoscopic techniques or open surgical procedures.

Fundamental knowledge of the airway can help to reduce the incidence of stenoses. The use of age-appropriate tubes and cuffless tubes, treatment of gastroesophageal reflux, and reducing the duration of mechanical ventilation have led to an overall decrease in laryngotracheal stenoses in the past decade.